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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1971 1
1976 1
1977 1
1978 3
1985 2
1986 1
1987 2
1988 10
1989 3
1990 5
1991 4
1992 10
1993 10
1994 16
1995 13
1996 8
1997 8
1998 13
1999 16
2000 14
2001 24
2002 16
2003 10
2004 17
2005 12
2006 16
2007 14
2008 14
2009 18
2010 11
2011 12
2012 18
2013 15
2014 17
2015 24
2016 19
2017 17
2018 7
2019 21
2020 23
2021 18
2022 10
2023 7
2024 5

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476 results

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Page 1
ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
Syngal S, Brand RE, Church JM, Giardiello FM, Hampel HL, Burt RW; American College of Gastroenterology. Syngal S, et al. Am J Gastroenterol. 2015 Feb;110(2):223-62; quiz 263. doi: 10.1038/ajg.2014.435. Epub 2015 Feb 3. Am J Gastroenterol. 2015. PMID: 25645574 Free PMC article. Review.
Genetic testing should be conducted in the context of pre- and post-test genetic counseling to ensure the patient's informed decision making. Patients who meet clinical criteria for a syndrome as well as those with identified pathogenic germline mutations should receive ap …
Genetic testing should be conducted in the context of pre- and post-test genetic counseling to ensure the patient's informed decision making …
Pathology and genetics of hereditary colorectal cancer.
Ma H, Brosens LAA, Offerhaus GJA, Giardiello FM, de Leng WWJ, Montgomery EA. Ma H, et al. Pathology. 2018 Jan;50(1):49-59. doi: 10.1016/j.pathol.2017.09.004. Epub 2017 Nov 21. Pathology. 2018. PMID: 29169633 Review.
Between 2 and 5% of all CRCs occur due to inherited syndromes, including Lynch syndrome, familial adenomatous polyposis, MUTYH-associated polyposis, Peutz-Jeghers syndrome, juvenile polyposis and Cowden/PTEN hamartoma syndrome. In addition, serrated po …
Between 2 and 5% of all CRCs occur due to inherited syndromes, including Lynch syndrome, familial adenomatous polyposis, MUTYH-associ …
Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Familial Tumor Syndromes.
Nosé V, Lazar AJ. Nosé V, et al. Head Neck Pathol. 2022 Mar;16(1):143-157. doi: 10.1007/s12105-022-01414-z. Epub 2022 Mar 21. Head Neck Pathol. 2022. PMID: 35312981 Free PMC article. Review.
This review highlights the important findings within these syndromes, especially on the update on syndromes with tumors involving the head and neck region, as Gorlin syndrome/nevoid basal cell carcinoma syndrome associated with odontogenic keratocysts; Brooke-Spiegl …
This review highlights the important findings within these syndromes, especially on the update on syndromes with tumors involving the head a …
An update on the CNS manifestations of neurofibromatosis type 2.
Coy S, Rashid R, Stemmer-Rachamimov A, Santagata S. Coy S, et al. Acta Neuropathol. 2020 Apr;139(4):643-665. doi: 10.1007/s00401-019-02029-5. Epub 2019 Jun 4. Acta Neuropathol. 2020. PMID: 31161239 Free PMC article. Review.
Neurofibromatosis type II (NF2) is a tumor predisposition syndrome characterized by the development of distinctive nervous system lesions. ...NF2 has a highly variable clinical course, with some patients exhibiting a severe phenotype and development of multiple tumo …
Neurofibromatosis type II (NF2) is a tumor predisposition syndrome characterized by the development of distinctive nervous system les …
Cowden syndrome and the PTEN hamartoma tumor syndrome: systematic review and revised diagnostic criteria.
Pilarski R, Burt R, Kohlman W, Pho L, Shannon KM, Swisher E. Pilarski R, et al. J Natl Cancer Inst. 2013 Nov 6;105(21):1607-16. doi: 10.1093/jnci/djt277. Epub 2013 Oct 17. J Natl Cancer Inst. 2013. PMID: 24136893 Review.
BACKGROUND: PTEN hamartoma tumor syndrome (PHTS) refers to a spectrum of disorders caused by mutations in the phosphatase and tensin homolog (PTEN) gene. ...RESULTS: We found no sufficient evidence to support inclusion of benign breast disease, uterine fibroi …
BACKGROUND: PTEN hamartoma tumor syndrome (PHTS) refers to a spectrum of disorders caused by mutations in the phosphatase and …
Lhermitte-Duclos disease: A case report and literature review.
Liu Z, He Y, Fu J, Wu J, Song T, Wang Y, Huang T. Liu Z, et al. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2021 Feb 28;46(2):195-199. doi: 10.11817/j.issn.1672-7347.2021.190574. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2021. PMID: 33678658 Free PMC article. Review. Chinese, English.
Lhermitte-Duclos disease (LDD) is a type of rare brain tumor located in posterior fossa. ...The pathogenesis, diagnosis and treatment of LDD are explored and summarized in combination with relevant literature. Lhermitte-Duclos disease (LD …
Lhermitte-Duclos disease (LDD) is a type of rare brain tumor located in posterior fossa. ...The pathogenesis, diagnosis …
Cowden Disease: A Review.
Magaña M, Landeta-Sa AP, López-Flores Y. Magaña M, et al. Am J Dermatopathol. 2022 Oct 1;44(10):705-717. doi: 10.1097/DAD.0000000000002234. Am J Dermatopathol. 2022. PMID: 36122333 Review.
PTEN hamartoma tumor syndrome (PTHS) includes diseases with germline pathogenic variants in the PTEN gene. ...Patients present benign and, malignant neoplasms in multiple organs, mostly breast and thyroid. The skin is the organ affected most consistently by C …
PTEN hamartoma tumor syndrome (PTHS) includes diseases with germline pathogenic variants in the PTEN gene. ...Patients present …
Dysmorphology.
Kim AY, Bodurtha JN. Kim AY, et al. Pediatr Rev. 2019 Dec;40(12):609-618. doi: 10.1542/pir.2018-0331. Pediatr Rev. 2019. PMID: 31792044 Review. No abstract available.
Lhermitte-Duclos Disease: A Rare Cerebellar Hamartoma Presenting Following Traumatic Brain Injury And A Review Of The Literature.
Ashraf M, Kamboh UA, Raza MA, Choudhary N, Mehboob M, Hussain SS, Ashraf N. Ashraf M, et al. J Ayub Med Coll Abbottabad. 2022 Jul-Sep;34(Suppl 1)(3):S733-S738. doi: 10.55519/JAMC-03-S1-9900. J Ayub Med Coll Abbottabad. 2022. PMID: 36414605 Free article. Review.
Lhermitte-Duclos Disease (LDD) is an extremely rare hamartoma of the cerebellum and is associated with the cancer syndrome Cowden's disease. We report such a patient whose disease was diagnosed incidental to traumatic brain injury. …
Lhermitte-Duclos Disease (LDD) is an extremely rare hamartoma of the cerebellum and is associated with the cance …
MR imaging features of Lhermitte-Duclos disease: Case reports and literature review.
Zhang HW, Zhang YQ, Liu XL, Mo YQ, Lei Y, Lin F, Feng YN. Zhang HW, et al. Medicine (Baltimore). 2022 Jan 28;101(4):e28667. doi: 10.1097/MD.0000000000028667. Medicine (Baltimore). 2022. PMID: 35089210 Free PMC article. Review.
RATIONALE: Lhermitte-Duclos disease (LDD) is a rare tumor of the nervous system with a typical "tiger striped'" sign, but its features on functional magnetic resonance imaging (fMRI) are still inconclusive. ...
RATIONALE: Lhermitte-Duclos disease (LDD) is a rare tumor of the nervous system with a typical "tiger striped'" sign, b …
476 results